Similar articles for PMID: 12812952

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1

Brain MR imaging in neonatal hyperammonemic encephalopathy resulting from proximal urea cycle disorders.

Takanashi J, Barkovich AJ, Cheng SF, Weisiger K, Zlatunich CO, Mudge C, Rosenthal P, Tuchman M, Packman S. Takanashi J, et al. AJNR Am J Neuroradiol. 2003 Jun-Jul;24(6):1184-7. AJNR Am J Neuroradiol. 2003. PMID: 12812952 Free PMC article.

2

Brain MR imaging in acute hyperammonemic encephalopathy arising from late-onset ornithine transcarbamylase deficiency.

Takanashi J, Barkovich AJ, Cheng SF, Kostiner D, Baker JC, Packman S. Takanashi J, et al. AJNR Am J Neuroradiol. 2003 Mar;24(3):390-3. AJNR Am J Neuroradiol. 2003. PMID: 12637287 Free PMC article.

3

Carbamyl phosphate synthetase 1 deficiency: a destructive encephalopathy.

Takeoka M, Soman TB, Shih VE, Caviness VS Jr, Krishnamoorthy KS. Takeoka M, et al. Pediatr Neurol. 2001 Mar;24(3):193-9. doi: 10.1016/s0887-8994(00)00259-9. Pediatr Neurol. 2001. PMID: 11301219

4

Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.

Pridmore CL, Clarke JT, Blaser S. Pridmore CL, et al. J Child Neurol. 1995 Sep;10(5):369-74. doi: 10.1177/088307389501000506. J Child Neurol. 1995. PMID: 7499756

5

Hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency due to a novel combined heterozygous mutations.

Gao J, Gao F, Hong F, Yu H, Jiang P. Gao J, et al. Am J Emerg Med. 2015 Mar;33(3):474.e1-3. doi: 10.1016/j.ajem.2014.08.038. Epub 2014 Aug 23. Am J Emerg Med. 2015. PMID: 25227973

6

Urea cycle disorders in Thai infants: a report of 5 cases.

Wasant P, Srisomsap C, Liammongkolkul S, Svasti J. Wasant P, et al. J Med Assoc Thai. 2002 Aug;85 Suppl 2:S720-31. J Med Assoc Thai. 2002. PMID: 12403252

7

Unfavorable clinical outcomes in patients with carbamoyl phosphate synthetase 1 deficiency.

Choi Y, Oh A, Lee Y, Kim GH, Choi JH, Yoo HW, Lee BH. Choi Y, et al. Clin Chim Acta. 2022 Feb 1;526:55-61. doi: 10.1016/j.cca.2021.11.029. Epub 2021 Dec 29. Clin Chim Acta. 2022. PMID: 34973183

8

The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation.

Kölker S, Garcia-Cazorla A, Valayannopoulos V, Lund AM, Burlina AB, Sykut-Cegielska J, Wijburg FA, Teles EL, Zeman J, Dionisi-Vici C, Barić I, Karall D, Augoustides-Savvopoulou P, Aksglaede L, Arnoux JB, Avram P, Baumgartner MR, Blasco-Alonso J, Chabrol B, Chakrapani A, Chapman K, I Saladelafont EC, Couce ML, de Meirleir L, Dobbelaere D, Dvorakova V, Furlan F, Gleich F, Gradowska W, Grünewald S, Jalan A, Häberle J, Haege G, Lachmann R, Laemmle A, Langereis E, de Lonlay P, Martinelli D, Matsumoto S, Mühlhausen C, de Baulny HO, Ortez C, Peña-Quintana L, Ramadža DP, Rodrigues E, Scholl-Bürgi S, Sokal E, Staufner C, Summar ML, Thompson N, Vara R, Pinera IV, Walter JH, Williams M, Burgard P. Kölker S, et al. J Inherit Metab Dis. 2015 Nov;38(6):1041-57. doi: 10.1007/s10545-015-9839-3. Epub 2015 Apr 15. J Inherit Metab Dis. 2015. PMID: 25875215

9

Parieto-occipital encephalomalacia in neonatal hyperammonemia with ornithine transcarbamylase deficiency: A case report.

Okanishi T, Ito T, Nakajima Y, Ito K, Kakita H, Yamada Y, Kobayashi S, Ando N, Togari H. Okanishi T, et al. Brain Dev. 2010 Aug;32(7):567-70. doi: 10.1016/j.braindev.2009.07.001. Epub 2009 Jul 28. Brain Dev. 2010. PMID: 19640662

10

Unmasked adult-onset urea cycle disorders in the critical care setting.

Summar ML, Barr F, Dawling S, Smith W, Lee B, Singh RH, Rhead WJ, Sniderman King L, Christman BW. Summar ML, et al. Crit Care Clin. 2005 Oct;21(4 Suppl):S1-8. doi: 10.1016/j.ccc.2005.05.002. Crit Care Clin. 2005. PMID: 16227111 Review.

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